Chapter 22: Problem 85
Polystyrene can be made more rigid by copolymerizing styrene with divinylbenzene: How does the divinylbenzene make the copolymer more rigid?
Chapter 22: Problem 85
Polystyrene can be made more rigid by copolymerizing styrene with divinylbenzene: How does the divinylbenzene make the copolymer more rigid?
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Get started for freeAspartame, the artificial sweetener marketed under the name NutraSweet, is a methyl ester of a dipeptide: a. What two amino acids are used to prepare aspartame? b. There is concern that methanol may be produced by the decomposition of aspartame. From what portion of the molecule can methanol be produced? Write an equation for this reaction.
Structural and optical isomers can be drawn having the formula \(\mathrm{C}_{5} \mathrm{H}_{11} \mathrm{F}\) . Give examples to illustrate these types of isomerism for \(\mathrm{C}_{5} \mathrm{H}_{11} \mathrm{F}\) . Why can't \(\mathrm{C}_{5} \mathrm{H}_{11} \mathrm{F}\) exhibit geometrical isomerism?
Consider a sample of a hydrocarbon at 0.959 atm and 298 K. Upon combusting the entire sample in oxygen, you collect a mixture of gaseous carbon dioxide and water vapor at 1.51 atm and 375 K. This mixture has a density of 1.391 g/L and occupies a volume four times as large as that of the pure hydrocarbon. Determine the molecular formula of the hydrocarbon and name it.
Why is glycine not optically active?
Ethylene oxide is an important industrial chemical. Although most ethers are unreactive, ethylene oxide is quite reactive. It resembles \(\mathrm{C}_{2} \mathrm{H}_{4}\) in its reactions in that addition reactions occur across the \(\mathrm{C}-\mathrm{O}\) bond in ethylene oxide. a. Why is ethylene oxide so reactive? (Hint: Consider the bond angles in ethylene oxide as compared with those predicted by the VSEPR model.) b. Ethylene oxide undergoes addition polymerization, forming a polymer used in many applications requiring a nonionic surfactant. Draw the structure of this polymer.
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